Publications by authors named "Yun-Gang Shen"

Given its unique function in light-induced water oxidation and its susceptibility to photoinactivation during photosynthesis, photosystem II (PS II) is often the focus of studies of photosynthetic structure and function, particularly in environmental stress conditions. Here we review four approaches for quantifying or monitoring PS II functionality or the stoichiometry of the two photosystems in leaf segments, scrutinizing the approximations in each approach. (1) Chlorophyll fluorescence parameters are convenient to derive, but the information-rich signal suffers from the localized nature of its detection in leaf tissue.

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Besides the non-cyclic electron transport driven by the two photosystems (PSII and PSI), the cyclic electron transport pathways around PSI are also essential for efficient photosynthesis. As one of these pathways, the NAD(P)H dehydrogenase complex (NDH complex) mediated cyclic electron transport has been well studied. Along with the identification of the plastid terminal oxydase (PTOX), the functions of NDH-mediated cyclic and chlororepiratory electron transport in energy supply for photosynthesis as well as in the resistance to photooxidative stress have increasingly been brought to the researchers' attention.

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State transition of the photosynthetic apparatus in plants is a short-term adaptation mediated mainly by the reversible phosphorylation of the main light-harvesting complex protein (LHCII) and its migration between photosystem I (PSI) and photosystem II (PSII). In higher plants and Chlamydomonas, LHCII phosphorylation is mainly controlled by the redox state of plastoquinone pool and cytochrome b(6)f complex, while salt could induce a redox-independent LHCII phosphorylation via transient changes in ion concentrations in Dunaliella. State transition can balance the distribution of excitation energy between PSII and PSI by changes in light absorption cross section and excitation energy spillover between the two photosystems.

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This study investigated the regulation of major light harvesting chlorophyll a/b protein (LHCII) phosphorylation by hypoosmotic shock in dark-adapted Dunaliella salina cells. When the external NaCl concentration decreased in darkness, D. salina LHCII phosphorylation levels transiently dropped within 20 min and then restored gradually to basal levels.

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The changes in trans-thylakoid membrane proton motive force caused by red light and caused by far-red light in the halotolerant green alga, Dunaliella salina are investigated. Irradiation with red light decreased the intensity of the fast phase of millisecond delayed light emission (ms-DLE) in D. salina, and far-red light led to the opposite effects.

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This study investigated the regulation of the major light harvesting chlorophyll a/b protein (LHCII) phosphorylation in Dunaliella salina thylakoid membranes. We found that both light and NaCl could induce LHCII phosphorylation in D. salina thylakoid membranes.

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Light could induce phosphorylation of light harvesting chlorophyll a/b binding proteins (LHCII) in Dunaliella salina and spinach thylakoid membranes. We found that neither phosphorylation was affected by glycerol, whereas treatment with NaCl significantly enhanced light-induced LHCII phosphorylation in D. salina thylakoid membranes and inhibited that in spinach.

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A successful study on the secondary structure of the isolated photosystem II (PSII) particles with the Fourier transform infrared spectroscopy is reported in this paper. The beta condensation effect is obviously characterized by infrared absorption spectra. The infrared spectra of both living protein and beta condensed protein samples are measured at room temperature.

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Many efforts have been paid to the separation of an integrated NA(D)PH dehydrogenase (NDH) complex. Several hydrophilic subcomplexes of NDH have been purified from the cyanobacterium Synechocystis PCC6803. However, no hydrophobic NDH subcomplex has ever been separated from cyanobacteria yet.

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Photoautotrophic carrot callus was induced by gradually lowering the sucrose concentration in culture medium. In the course of induction, the net photosynthetic rate on chlorophyll basis of callus increased gradually with the decreasing of sucrose concentration in culture medium, and the net photosynthetic rate of photoautotrophic callus could even be higher than that of leaf. In the course of changing into photoautotrophic callus, its chlorophyll content increased gradually, and the dark respiratory rate and the ratio of Chl a/Chl b decreased gradually.

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The reaction centers are isolated from chromatophores of Rhodobacter sphaeroides 601 by detergent LDAO, and purified by chromatography on a DEAE-52 cellulose column. In the presence of acetone and an access of free pheophytins (Phes), bacteriopheophytins (Bphes) in reaction centers are replaced by pheophytins at sites H(A) and H(B) when incubated under high temperature. The substituting amounts are about 50% and 71% Bphes in reaction centers with incubation of fifteen and sixty minutes respectively.

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2,5 dibromo-3-methyl-5-isopropyl-p-benzoquinone (DBMIB), an inhibitor of plastoquinone, inhibited photosystem I cyclic electron transport mediated by pyocyanine of low concentration, but had no effect on that mediated by phenazine methosulphate (PMS). In the presence of pyocyanine, the thylakoids displayed a transient post-illumination increase in chlorophyll fluorescence which resembled that displayed in leaves. The above results indicate the involvement of plastoquinone in the pyocyanine-mediated cyclic electron transport around photosystem I.

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The entire atpE gene of the maize chloroplast coupling factor was inserted into the polylinker region of vectors pJLA505 and pWA to form recombinant plasmids pJLA505-atpE and pWA-atpE respectively. These expression plasmids were transformed into E. coli NM522 which induced at 42 degrees.

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